warnings
WARNINGS:
Mucus Relief DM
openFDA label record#
This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.
Verified complete openFDA source JSON
- Brand name
- Mucus Relief DM
- Generic name
- DEXTROMETHORPHAN HBR 20MG GUAIFENESIN 400MG
- Manufacturer
- NUVICARE LLC
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 6c4bc7d1-09d9-4311-8457-a1d47ab02a5a
- SPL ID
- ebde3135-67a7-4d03-a94a-4df3f9474c6b
- Version
- 1
- Effective date
- 2026-03-05
- Source export date
- 2026-09-28
- Source partition
- 10
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0010-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/4bbc9760f647649b787710953d978bd6419e899ba8b90f32c3d972aae43947f8/drug-label-0010-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 06:06:19
| Harmonized routes |
|---|
| ORAL |
Harmonized identifier links#
Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.
| Type | Scope | Identifier | Source field |
|---|---|---|---|
| application number | M012 | openfda.application_number | |
| brand name | Mucus Relief DM | openfda.brand_name | |
| generic name | DEXTROMETHORPHAN HBR 20MG GUAIFENESIN 400MG | openfda.generic_name | |
| manufacturer name | NUVICARE LLC | openfda.manufacturer_name | |
| ndc | package | 84324-035-01 | openfda.package_ndc |
| ndc | product | 84324-035 | openfda.product_ndc |
| ndc11 | package | 84324003501 | derived:openfda.package_ndc |
| rxcui | 1147685 | openfda.rxcui | |
| spl id | ebde3135-67a7-4d03-a94a-4df3f9474c6b | id | |
| spl set id | 6c4bc7d1-09d9-4311-8457-a1d47ab02a5a | set_id | |
| unii | 9D2RTI9KYH | openfda.unii | |
| unii | 495W7451VQ | openfda.unii |
Warnings cross-check#
openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.